K-number	K050136
Device name	REPROCESSED HOT BIOPSY FORCEPS
Applicant	Sterilmed, Inc.
Product code	NLU
Device class	Class II
Decision date	Jul 20, 2005
Decision	Substantially Equivalent
Regulation	876.4300

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View the full FDA submission: accessdata.fda.gov

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REPROCESSED HOT BIOPSY FORCEPS

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